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1.
Ann Med Surg (Lond) ; 81: 104503, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-36147051

RESUMO

Background: When evaluating trauma patients, many centers perform computed tomography of the head, cervical spine, chest, abdomen, and pelvis, the so-called "pan-scan." Here, we evaluate the utility of physical exam against pan-scan in geriatric patients who sustained ground-level falls. Methods: We performed a single-centered retrospective cohort review of consecutive patients from the trauma registry of a large, urban Level 1 trauma center. Inclusion criteria were registration during the 2019 calendar year, age ≥65, mechanism of fall from either sitting or standing, and performance of "pan-scan" at time of assessment. The sensitivity, specificity, positive and negative predictive values of the physical exam for significant injuries were calculated. The effect of such injuries on disposition from the emergency department and hospital were determined. Results: An initial query for patients age ≥65 yielded 1280 patients. After exclusion of patients who did not undergo pan-scan or who had GCS <14, 751 patients were included in analysis. Median age was 84 years old. 351 patients had at least one injury identified on pan-scan. Physical exam was determined to have a sensitivity of 0.69 when compared to pan-scan as a gold standard. Patients with injury identified on CT scan had significantly more admissions, mortalities, and ICU and OR requirements. Conclusion: Approximately half of all patients were found to have at least one injury on pan-scan. Physical examination was insensitive at identifying such injuries which ultimately altered patient management, disposition, and outcomes. Pan-scan is recommended in this vulnerable population.

2.
Br J Dermatol ; 174(6): 1299-307, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26799159

RESUMO

BACKGROUND: Acne vulgaris is a multifactorial disorder of the pilosebaceous units. Several studies have reported that insulin-like growth factor (IGF)-1, forkhead box transcription factor (Fox)O1 and mammalian target of rapamycin (mTOR) interactions may be the key to understanding the links between genetic and environmental factors in acne vulgaris. OBJECTIVES: To evaluate the immunohistochemical detection of mTOR and FoxO1 in the skin, and the serum level of IGF-1 in patients with acne vulgaris. METHODS: This study was carried out on 60 participants, including 40 patients with acne and 20 controls. A diet questionnaire was administered to the patients and controls. Serum levels of IGF-1 were measured using enzyme-linked immunosorbent assay, and skin biopsies were taken from lesions on the backs of the patients and controls. FoxO1 and mTOR expression was detected using immunohistochemistry. RESULTS: A significantly higher serum IGF-1 level was found in the patients with acne than in the controls. The cytoplasmic expression of FoxO1 was found to be significantly greater in the acne group, whereas in the control subjects this expression was likely to be nuclear. Both the cytoplasmic expression and the nuclear expression of mTOR were significantly more intense in the patients with acne than in the controls. Excess consumption of a high-glycaemic-load diet was significantly associated with higher serum levels of IGF-1 and cytoplasmic expression of FoxO1 and mTOR. CONCLUSIONS: These results suggest that FoxO1, mTOR, serum IGF-1 and a high-glycaemic-load diet may play a role in acne pathogenesis.


Assuntos
Acne Vulgar/etiologia , Dieta/efeitos adversos , Fatores de Transcrição Forkhead/metabolismo , Fator de Crescimento Insulin-Like I/metabolismo , Serina-Treonina Quinases TOR/metabolismo , Acne Vulgar/metabolismo , Adulto , Estudos de Casos e Controles , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Imuno-Histoquímica , Estilo de Vida , Masculino , Pele/metabolismo , Adulto Jovem
3.
Transfus Med ; 25(6): 380-4, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26578338

RESUMO

OBJECTIVES: To document the incidence of lymphocytotoxic antibodies (LCA) in chronically transfused children with ß thalassemia major and the relationship between alloimmunisation and febrile non-haemolytic transfusion reactions. We also compared the effect of leucoreduced-packed red blood cells (RBCs) by bed-side filtration and washed RBCs in preventing FNHTRs and in inducing haemoglobin rise. BACKGROUND: Alloimmunisation to human leucocytic antigens is one of the common complications of transfusions, particularly in chronically transfused patients as those with thalassemia major, a common disease in Northern Egypt. METHODS/MATERIALS: LCA were screened for in 45 chronically transfused ß thalassemia major children (group I), 20 splenectomised ones (group II) and 20 healthy controls (group III), using qualitative lymphocytotoxic antibody (LCA) enzyme-linked immunosorbent assay (ELISA) kit. RESULTS: Nine out of 65 thalassemic children (∼14%) were positive for LCA antibodies. Frequency of transfusions and LCA positivity were significantly higher in group I than group II (p = 0.036 and 0.014). There was no statistically significant difference between LCA positive and negative cases regarding age of starting transfusion, frequency of transfusions or FNHTRs. There was no statistically significant difference between washed and filtered RBCs in reducing FNHTRs (p = 1.000) and in inducing haemoglobin rise in positive LCA cases (p = 0.409). CONCLUSION: Human leukocyte antigen (HLA) alloimmunisation was only 14% in the children with ß thalassemia major we studied. Surprisingly FNHTRs were not more common in those with HLA antibodies. Splenectomy plays a role in reducing the frequency of transfusion and HLA alloimmunisation. Washed and filtered RBCs are comparable in reducing FNHTRs and in inducing haemoglobin rise.


Assuntos
Transfusão de Eritrócitos/efeitos adversos , Antígenos HLA/imunologia , Isoanticorpos , Criança , Pré-Escolar , Egito , Feminino , Humanos , Lactente , Isoanticorpos/sangue , Isoanticorpos/imunologia , Masculino , Talassemia beta/sangue , Talassemia beta/imunologia , Talassemia beta/terapia
4.
Andrologia ; 47(2): 228-35, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24571379

RESUMO

Chromosome anomalies were suggested to be more frequent in infertile males so our case-control study aimed at evaluating the incidence of spermatic aneuploidies in forty males with severe oligoasthenoteratozoospermia (OAT) and comparing it with that in another forty males having normal semen parameters. Semen samples were collected and analysed in the Clinical Pathology Department according to criteria of the World Health Organization (WHO laboratory manual for the examination and processing of human semen, 2010, WHO Press). Fluorescence in situ hybridisation (FISH) was performed on decondensed spermatozoa from fresh semen ejaculates, using dual coloured chromosome-specific DNA probes labelled with fluorochromes to study sperm aneuploidies in chromosomes 13, 21, X and Y. There was no statistical significant difference between cases and controls regarding disomy frequencies for chromosomes 13, 21 or both combined. However, 13, 21 diploidy frequency was significantly higher among OAT cases. Regarding chromosomes X and Y, both cases and controls showed similar results for disomy/diploidy frequency for both chromosomes; however, there was a statistical significant increase in YY disomy/diploidy frequency among OAT patients. X chromosome-bearing spermatozoa were found to be significantly higher among controls. Patients with severe OAT have a higher total sperm aneuploidy rate, regarding chromosomes 13, 21, X and Y but without a statistical significant difference.


Assuntos
Aneuploidia , Azoospermia/genética , Hibridização in Situ Fluorescente/métodos , Infertilidade Masculina/genética , Análise do Sêmen/métodos , Espermatozoides/patologia , Adulto , Azoospermia/etnologia , Azoospermia/patologia , Estudos de Casos e Controles , Cromossomos Humanos Par 13/genética , Cromossomos Humanos Par 21/genética , Cromossomos Humanos X/genética , Cromossomos Humanos Y/genética , Egito , Humanos , Incidência , Infertilidade Masculina/etnologia , Infertilidade Masculina/patologia , Masculino , Pessoa de Meia-Idade
5.
Andrologia ; 47(9): 1028-33, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25351208

RESUMO

Germ cell apoptosis has been proposed as one of the mechanisms by which varicocele can influence fertility. The aim of this study was to investigate the relationship between seminal tumour necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) levels and male infertility in patients with varicocele. This study included 112 males: 30 fertile males with varicocele, 44 infertile males with varicocele and 38 healthy fertile control subjects without varicocele. Semen analysis was performed, and serum levels of reproductive hormones were measured. Seminal TRAIL levels in the infertile varicocele group were significantly higher than in the fertile varicocele and the control groups (P = 0.014). A significant negative correlation was found between seminal TRAIL and progressive (P < 0.001) and total motility scores (P < 0.001) in the infertile varicocele group. A significant negative correlation was also detected between seminal TRAIL levels and normal sperm morphology in the fertile varicocele (P = 0.007) and infertile varicocele patients (P = 0.047). Seminal TRAIL was significantly correlated with varicocele grade whether the patients were fertile (P = 0.001) or infertile (P = 0.035). Seminal TRAIL may thus have a potential role in varicocele-associated male infertility through its negative effect on sperm motility and morphology.


Assuntos
Apoptose , Infertilidade Masculina/metabolismo , Sêmen/metabolismo , Ligante Indutor de Apoptose Relacionado a TNF/metabolismo , Varicocele/metabolismo , Adulto , Estudos de Casos e Controles , Egito , Hormônio Foliculoestimulante/sangue , Humanos , Infertilidade Masculina/complicações , Hormônio Luteinizante/sangue , Masculino , Pessoa de Meia-Idade , Análise do Sêmen , Testosterona/sangue , Varicocele/complicações , Adulto Jovem
6.
Am J Transplant ; 6(9): 2212-7, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16780542

RESUMO

Nephrogenic systemic fibrosis (NSF) is a recently characterized systemic fibrosing disorder developing in the setting of renal insufficiency. NSF's rapidly progressive nature resulting in disability within weeks of onset makes early diagnosis important. Two reports of NSF after liver transplantation are known of. We present three cases of NSF developing within a few months after liver transplantation and review the current literature. Loss of regulatory control of the circulating fibrocyte, its aberrant recruitment, in a milieu of renal failure and a recent vascular procedure appear important in its development. Known current therapies lack consistent efficacy. Only an improvement in renal function has the greatest likelihood of NSF's resolution. Delayed recognition may pose a significant barrier to functional recovery in the ubiquitously deconditioned liver transplant patient. Early recognition and implementation of aggressive physical therapy appear to have the greatest impact on halting its progression.


Assuntos
Nefropatias/etiologia , Transplante de Fígado/efeitos adversos , Dermatopatias/etiologia , Idoso , Fibrose/etiologia , Humanos , Nefropatias/patologia , Nefropatias/terapia , Masculino , Pessoa de Meia-Idade , Dermatopatias/patologia , Dermatopatias/terapia , Resultado do Tratamento
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